EP0232596A1 - Liquid applicator - Google Patents
Liquid applicator Download PDFInfo
- Publication number
- EP0232596A1 EP0232596A1 EP86308960A EP86308960A EP0232596A1 EP 0232596 A1 EP0232596 A1 EP 0232596A1 EP 86308960 A EP86308960 A EP 86308960A EP 86308960 A EP86308960 A EP 86308960A EP 0232596 A1 EP0232596 A1 EP 0232596A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- applicator
- elongate member
- liquid
- hollow elongate
- porous
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000007788 liquid Substances 0.000 title claims abstract description 45
- 239000000463 material Substances 0.000 claims abstract description 32
- 239000011148 porous material Substances 0.000 claims description 16
- 239000011800 void material Substances 0.000 claims description 12
- 230000006835 compression Effects 0.000 claims description 10
- 238000007906 compression Methods 0.000 claims description 10
- 229920001903 high density polyethylene Polymers 0.000 claims description 3
- 239000004700 high-density polyethylene Substances 0.000 claims description 3
- 230000001105 regulatory effect Effects 0.000 claims description 2
- 239000006260 foam Substances 0.000 abstract description 30
- 239000003973 paint Substances 0.000 abstract description 3
- 238000009736 wetting Methods 0.000 abstract description 3
- 239000000243 solution Substances 0.000 description 21
- 239000012530 fluid Substances 0.000 description 18
- 230000002421 anti-septic effect Effects 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000002184 metal Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- -1 polypropylene Polymers 0.000 description 5
- 229920001169 thermoplastic Polymers 0.000 description 5
- 239000004416 thermosoftening plastic Substances 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 239000012528 membrane Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000001356 surgical procedure Methods 0.000 description 3
- 239000012815 thermoplastic material Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 239000006261 foam material Substances 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 230000001939 inductive effect Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000004831 Hot glue Substances 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 208000003629 Rupture Diseases 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229940058401 polytetrafluoroethylene Drugs 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M35/00—Devices for applying media, e.g. remedies, on the human body
- A61M35/003—Portable hand-held applicators having means for dispensing or spreading integral media
- A61M35/006—Portable hand-held applicators having means for dispensing or spreading integral media using sponges, foams, absorbent pads or swabs as spreading means
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D47/00—Closures with filling and discharging, or with discharging, devices
- B65D47/42—Closures with filling and discharging, or with discharging, devices with pads or like contents-applying means
Definitions
- This invention relates to liquid applicators having particular utility in the field of aseptic surgery preparation. More particularly, this invention relates to articles useful in applying pre-operative surgical scrubs or paints to skin.
- Antiseptic preparation of patients for surgery conventionally includes a 3-l0 minute scrubbing of the affected area with a soap solution followed by the application of a water-soluble antiseptic paint solution. These solutions are generally applied with saturated sponges that are attached to a blade or held with forceps. The sponges are saturated by soaking in open pans of solution. Numerous devices have been developed in an attempt to prevent the dripping of solution associated with the original technique. Another goal was to reduce the time required for application of the antiseptic solution.
- U.S. Patent Nos. 4,4l5,288; 4,507,lll; and 4,498,796 describe a device that includes a liquid-containing rupturable cylindrical cartridge which is slidable within a tubular handle having one or two hollow interior spikes.
- the spikes communicate to recesses bored or burned into the interior of the sponge to facilitate free flow and even distribution of the fluid.
- air In order for fluid to flow by gravity from this device, air must be entrained into the cartridge through the sponge and at least one hollow spike. For the following two reasons, this is not a reliable and predictable means to control the rate of delivery of fluid to the sponge.
- the device described in U.S. Patent 3,847,l5l includes a sponge mounted on a nozzle extending from a hollow handle which contains an antiseptic solution.
- the solution is dispensed into the sponge when a rupturable joint in the nozzle is broken and external pressure is applied to the flexible handle.
- the problems associated with the design of this device include the unreliability of the rupturable joint and the lack of control of the fluid delivery into the sponge.
- Inherent mass production variability makes the fabrication of a reliable rupturable joint based on stress concentration difficult. After the nozzle is opened, it is very difficult, in practice, to deliver precisely the correct volume of fluid to saturate the sponge without dripping. In addition, as the sponge is wetted by the fluid, its ability to entrain air is diminished.
- U.S. Patent 4,l48,3l8 describes a device that includes an antiseptic solution contained in an integral reservoir with a frangible cover. Spikes affixed to a recess in the sponge pierce the cover to release the solution.
- the disadvantage of this device and other devices that include liquid-containing ampoules, such as those described in U.S. Patent Nos. 3,89l,33l and 4,l83,684, is the absence of a means to control the delivery of fluid to the sponge. The absence of a means to control the fluid flow rate to the sponge limits the volume of solution that can be delivered without dripping.
- U.S. Patent No. 4,342,522 describes a roll-on dispenser which includes a porous open-cell foam membrane deformable by an applicator ball to regulate the dispensation of controlled amounts of powders.
- the amount of material dispensed is dependent upon the porosity of the membrane and the porosity of the membrane is dependent upon the degree of its deformation by the ball upon operation of the dispenser.
- This invention relates to an article useful as a dispenser for the application of a liquid to a surface comprising
- the current invention provides a means to reliably deliver in a short period of time a surgical prep solution to an applicator sponge without dripping.
- the applicator of the present invention controls the flow rate of liquid therein to the applicator sponge without the need for external operator manipulation.
- the applicator of this invention provides control of the flow rate of liquid to the applicator sponge without squeezing the liquid container or compressing the applicator sponge.
- this device can be configured to apply a variety of solution compositions, viscosities and volumes without compromising the fast wetting and no dripping features.
- the geometry of the device was designed to be compatible with modern antiseptic techniques. Because fabrication of the device utilizes high volume production processes, the manufacturing costs of the device are sufficiently inexpensive to permit disposable use.
- the applicator 30 includes a reservoir l containing the solution to be applied by the applicator, and a hollow elongate member 24 which acts as a handle and a conduit through which the solution passes before it is dispensed by foam sponge 8.
- hollow elongate member 24 is bounded by major orifice ll at one end and flange at the opposite end. It is constructed so as to include a fixation means 4 adjacent orifice ll for engaging at orifice ll reservoir l, a tubular handle 3 communicating between major orifice ll and major orifice 20 defined by flange 5, and an air vent 9. Air vent 9 aspirates air into hollow elongate member 24 as liquid flows out through major orifice 20 during the dispensation process, thereby maintaining atmospheric pressure inside the applicator.
- a porous metering insert 6 is disposed over major orifice 20 and is sandwiched between the underside of flange 5 and open-cell foam sponge 8.
- the porous metering insert 6 is disposed over major orifice 20 to control the flow of liquid out of hollow elongate member 24 and into foam sponge 8.
- Foam sponge 8 can be selected from a variety of commercially available materials having a wide range of compression set ratios (i.e., density) and porosities. By varying the pore size, void fraction and hydrophilicity of the porous metering insert 6 and the compression set ratio and porosity of the foam sponge 8, applicators can be constructed to apply a variety of solution compositions, viscosities and volumes.
- the pore size, void volume fraction, and hydrophilicity of porous metering material 6 and the compression set ratio and porosity of open-cell foam sponge 8 are adjusted in relation to the viscosity, volume and surface tension of the liquid to be dispensed to allow a portion of the liquid contained in the applicator to flow to the outer surface of sponge 8 but not to allow the liquid to drip from the open-cell foam sponge 8 when it is suspended in mid-air with flange 5 down. It should be noted that to create a completely dripless applicator the amount of liquid to be dispensed by the device must not exceed the reservoiring capacity of sponge 8.
- Metering insert 6 and sponge 8 are held together and disposed over major orifice 20 by a variety of suitable means, including adhesive bonding.
- elongate member 24 includes a flange 5 surrounding major orifice 20.
- the inner portion of flange 5 contains two lips defined by recesses l3 and l4.
- Metering insert 6 is contained within recess l3 and is held therein by foam sponge insert 8 which is adhered to the outer rim of flange 5 by heat-activatable bonding insert 7.
- Figure l shows the preferred embodiment fully assembled from each of the parts shown in Figure 2.
- the device illustrated in Figure l consists of the following components as shown in Figure 2: reservoir l containing the prep solution and sealed at its major orifice 2l by seal 2; hollow elongate member 24 being threaded at one end to accept reservoir l, and having an angled flange 5 at the opposite end, and including air vent 9; porous metering insert 6 disposed within flange 5; thermoplastic bonding insert 7 also disposed within flange 5; and foam sponge 8.
- Reservoir l is preferably a bottle with a threaded opening molded from a thermoplastic material compatible with the prep solution.
- the preferred embodiment comprises an essentially rigid, high-density polyethylene, cylindrical bottle with threaded portion l0 smaller in diameter than the main body of the bottle.
- Reservoir l is preferably filled and inductively sealed with foil seal 2 using conventional techniques.
- Hollow elongate member 24 can be molded from any thermoplastic compatible with the liquid to be dispensed.
- hollow elongate member 24 is molded from medium density polyethylene.
- this component include tubular handle 3, major orifice ll which communicates with reservoir l at orifice 2l thereof, integrally-formed radially-projecting interior flange l2 which acts as a reservoir seat, integrally-formed fixation means 4 which threadably engages reservoir l, projecting means l9 to tear seal 2 on reservoir l, air vent 9, and flange 5 located at the opposite end of hollow elongate member 24 from orifice ll.
- tubular handle 3 be long enough to prevent contact of the patient by the person applying the surgical prep solution.
- tubular handle 3 is at least about four inches long.
- Projecting means l9 is positioned within hollow elongate member 24 so as to be capable of puncturing seal 2 on reservoir l when reservoir l is engaged at orifice ll by fixation means 4.
- the preferred embodiment includes an integrally-formed projection that first extends radially from integrally-formed radially-projecting interior flange l2 and then extends in a direction towards orifice ll, parallel to the longitudinal axis of elongate member 24.
- the projection l9 is preferably of a size sufficient to begin rupturing seal 2 after reservoir l has been threaded at least one-half turn into hollow elongate member 24, with complete rupturing occuring three-fourth turn thereafter.
- Other possible embodiments of projecting means l9 include a hollow metal or polymeric spike.
- Air vent 9 is a necessary component of the applicator.
- Metering insert 6 greatly restricts the amount of air which can enter the applicator through orifice 20.
- Air vent 9 provides such a means.
- Air vent 9 is preferively an L-shaped slot having its long leg lying parallel to the longitudinal axis of elongate member 24 and recessed through the threads of fixation means 4, and its short leg lying perpendicular to the longitudinal axis of elongate member 24 and recessed through an upper portion of interior flange l2.
- air vent 9 is located on the wall of hollow elongate member 24 which forms an obtuse angle with flange 5.
- the short leg of air vent 9 projects only through an upper portion of flange l2, leaving the lower portion of this flange intact and radially projecting into the interior of elongate member 24.
- the liquid cascades over flange l2 and past air vent 9, thereby minimizing the potential for leakage of liquid through air vent 9.
- the size of air vent 9 is minimized.
- air vent 9 could merely comprise a hole through tubular handle 3. Preferably such a hole would not be present in a location which would result in leakage of liquid from the device.
- flange 5 is integrally formed and is angled from the longitudinal axis of elongate member 24 by between about 30 and 90 degrees. Most preferably there is about a 45 degree angle between flange 5 and the longitudinal axis of elongate member 24.
- Flange 5 preferably includes recesses l3 and l4 on its interior surface. Recesses l3 and l4 are dimensioned and shaped to permit nesting therein of metering insert 6 and bonding insert 7, respectively.
- recess l4 is greater in area than recess l3 to provide for sandwiching of metering insert 6 between orifice 20 and bonding insert 7.
- the distribution and rate of delivery of the liquid to open-cell foam sponge 8 is controlled by porous metering insert 6.
- porous metering insert 6 For a given volume, viscosity, and surface tension of the liquid, rapid wetting of the foam sponge without dripping can be accomplished by appropriate specification of the average pore size, void volume fraction and hydrophilicity of porous metering insert 6 and the permanent compression set ratio and porosity of open-cell foam sponge 8.
- the pore size, void volume and hydrophilicity of porous metering insert 6 are adjusted so that for any given volume, viscosity and surface tension of the liquid to be applied the average flow rate of the liquid through metering insert 6 is between about 0.25 and l0 mls/sec. Greater flow rates than this will tend to result in an applicator which drips, while lower flow rates will result in an applicator which does not provide adequate liquid for surgical scrub applications. Most preferably for surgical scrub applications, the average flow rate of liquid through porous metering insert 6 is between l and 5 ml/sec.
- porous metering insert 6 In general, for lower volumes and/or higher viscosity liquids the pore size and/or void volume of porous metering insert 6 is adjusted upwards to achieve the desired flow rates. Furthermore, as the surface tension of the liquid increases the metering insert is varied from a hydrophobic to a hydrophilic material to achieve the desired flow rate.
- Porous metering insert 6 is substantially rigid and can be constructed from either hydrophilic or hydrophobic materials depending upon the liquid to be dispensed.
- Metering insert 6 can be in the form of sintered metal or plastic, molded unfoamed porous plastic, porous plastic films, porous metal structures and porous ceramics. Methods for making such porous structures include well-known sintering or leaching processes.
- porous metering inserts are constructed from ceramics or thermoplastic materials such as polypropylene, polyethylene, polyvinylidene fluoride, ethylene-vinyl acetate copolymers, styrene-acrylonitrile copolymers and polytetrafluoroethylene.
- the hydrophilicity of the metering insert can be increased by various well-known treatments.
- the average pore size of metering insert 6 is between about l and 2,000 microns and the void volume is between about l0 and 70 percent.
- the average pore size of the metering insert is between about l0 and 500 microns and the void volume is between about 20 and 60 percent.
- the average pore size is between about 60 and l00 microns and the void volume is between about 30 and 50 percent.
- a preferred ceramic material for use as a porous metering insert is 3M Brand Porous StructuresTM, commercially available from 3M, Saint Paul, Minnesota.
- This material has an average pore size of between about l4 and l75 microns and a void volume of approximately 30 percent.
- a particularly preferred porous metering material is a porous high density polyethylene commercially available as Interflo® Porous Plastic, F/N35-l60-22, from Chromex Chemical Corp., Brooklyn, New York. This material has an average pore size of between about 60 and l00 microns and a void volume of between about 40 and 60 percent.
- metering insert 6 is relatively non-reservoiring, having a reservoiring capacity of less than about 5.0 cc/gm, preferably less than about l.0 cc/gm, and most preferably about 0.7 cc/gm. Fluid which is reservoired in an intermediate flow regulator is not available for application to the surface to be treated. Thus, metering insert 6 provides controlled flow of fluid without significant fluid waste due to retained fluid within the metering insert itself.
- the preferred embodiment of porous metering insert 6 has an area which is greater than the area of major orifice 20.
- the area of insert 6 is at least two times greater than the area of orifice 20, and is most preferably almost as large as foam sponge 8.
- the preferred embodiment of metering insert 6 also has a raised periphery l6 which extends above planar metering area l5 and creates a cavity between active metering area l5 and major orifice 20.
- raised periphery l6 extends above planar metering area l5 to the extent of one to two times the thickness of planar metering area l5. Both the increased area of insert 6 and raised periphery l6 serve to increase the area of fluid distribution to open-cell foam sponge 8.
- Bonding insert 7 is a gasket-like structure, preferably having a rectangular annular shape.
- a bridging member 22 is included between opposing sides of bonding insert 7 to provide stuctural support to foam sponge 8 and prevent sagging thereof due to the weight of the absorbed fluid to be dispensed.
- metering insert 6 and foam sponge 8 are peripherally affixed to flange 5 by bond l7, and metering insert 6 and foam sponge 8 are bonded together at bond l8.
- Bonding insert 7 can be molded, extruded or die cut from a compatible thermoplastic or heat-activatable material filled with an inductively active material.
- examples include laminated composites comprised of metal foil sandwiched between layers of thermoplastic or heat-activatable bonding material, such as polyethylene or hot-melt adhesives.
- Preferred examples include such thermoplastic or heat-activatable bonding materials filled with an inductive metal or metal oxide powder, e.g., 5 to 50 percent by volume iron powder having an average particle size of from about 300 to 400 mesh.
- a particularly preferred bonding insert 7 is a rigid gasket formed from injection molded polyethylene filled with about l2 to l5 percent by volume iron powder, commercially available from Emabond Inc., Norwood, New Jersey, as G-l0-205.
- Open-cell foam sponge 8 comprises an open-cell foam material compatible with the liquid to be dispensed.
- Suitable open-cell foam sponge materials are prepared from elastomeric thermoplastic materials such as polyethylene and polyurethane.
- Especially preferred open-cell foam materials are prepared from polyurethane elastomers.
- the wicking and reservoiring properties of the foam sponge 8 can be selected such that the fluid delivered through metering insert 6 wets foam sponge 8 but does not drip from sponge 8 when it is suspended in mid-air with flange 5 down.
- the greater the compression set ratio the greater the amount of liquid that can be absorbed by the sponge material.
- the foam sponge material is compression set (i.e., compressed) by heat and pressure to from about l.5 to l0 times its original density, i.e., the compression set ratio is between about l.5 and l0.
- the compression set ratio of sponge 8 is between about 2 and 4.
- the porosity of the foam sponge material can be selected such that foam sponge 8 will release a uniform amount of liquid when it is lightly rubbed against the surface upon which the liquid is to be dispensed.
- the porosity of the foam sponge material is between about l0 and l00 pores per linear inch, more preferably about 90 pores per linear inch.
- a particularly preferred open-cell foam sponge material is an elastomeric polyurethane foam having a compression set ratio of between about 2 and 4 and a porosity of about 90 pores per linear inch, commercially available from Scotfoam Corp., Eddystone, Pennsylvania, as ScottfeltTM 3-900-Z.
- the applicator of this invention is useful in dispensing liquids having viscosities at ambient temperatures of less than about l0,000 cps, most preferively less than about 500 cps.
- the applicator is useful in dispensing antiseptic liquids to cleanse a surgical field prior to surgery.
- suitable antiseptic preparations include those described in U.S. application Serial No. 6l7,255, filed June 4, l984, and those described in U.S. 4,542,0l2, the disclosures of which are incorporated herein by reference.
- the antiseptic liquid is placed in the applicator and the applicator head is gently rubbed over the surgical field to thereby cleanse it.
- the applicator can be handled easily without dripping the liquid onto other articles in the vicinity of the surgical field.
- the dripless feature allows application of the liquid to only the desired areas of the patient and also allows for quicker and more efficient use of a surgical facility due to elimination of the time needed to clean the facility of the drippings of antiseptic prep.
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Anesthesiology (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Mechanical Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Media Introduction/Drainage Providing Device (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
Abstract
Description
- This invention relates to liquid applicators having particular utility in the field of aseptic surgery preparation. More particularly, this invention relates to articles useful in applying pre-operative surgical scrubs or paints to skin.
- Antiseptic preparation of patients for surgery conventionally includes a 3-l0 minute scrubbing of the affected area with a soap solution followed by the application of a water-soluble antiseptic paint solution. These solutions are generally applied with saturated sponges that are attached to a blade or held with forceps. The sponges are saturated by soaking in open pans of solution. Numerous devices have been developed in an attempt to prevent the dripping of solution associated with the original technique. Another goal was to reduce the time required for application of the antiseptic solution.
- The most important problem associated with prior art devices developed to apply surgical prep solutions is the lack of control of the delivery of the fluid to the sponge in a manner that will prevent dripping. Additional problems encountered with such devices include manufacturing complexity, reliability of rupturable joints and inappropriate geometries.
- U.S. Patent Nos. 4,4l5,288; 4,507,lll; and 4,498,796 describe a device that includes a liquid-containing rupturable cylindrical cartridge which is slidable within a tubular handle having one or two hollow interior spikes. In the device of U.S. Patent No. 4,498,796, the spikes communicate to recesses bored or burned into the interior of the sponge to facilitate free flow and even distribution of the fluid. In order for fluid to flow by gravity from this device, air must be entrained into the cartridge through the sponge and at least one hollow spike. For the following two reasons, this is not a reliable and predictable means to control the rate of delivery of fluid to the sponge. First, as the sponge becomes wet its air permeability decreases thereby restricting the entrainment of air. Second, hollow tubes with sufficiently small inside diameters to effectively meter the fluid flow rate to prevent dripping tend to "air-lock" due to the surface tension of the liquid. An additional disadvantage of the design of this device is the recesses in the sponge. These recesses are an attempt to improve the predictability of air entrainment and fluid distribution, but add to the manufacturing costs.
- The device described in U.S. Patent 3,847,l5l includes a sponge mounted on a nozzle extending from a hollow handle which contains an antiseptic solution. The solution is dispensed into the sponge when a rupturable joint in the nozzle is broken and external pressure is applied to the flexible handle. The problems associated with the design of this device include the unreliability of the rupturable joint and the lack of control of the fluid delivery into the sponge. Inherent mass production variability makes the fabrication of a reliable rupturable joint based on stress concentration difficult. After the nozzle is opened, it is very difficult, in practice, to deliver precisely the correct volume of fluid to saturate the sponge without dripping. In addition, as the sponge is wetted by the fluid, its ability to entrain air is diminished.
- U.S. Patent 4,l48,3l8 describes a device that includes an antiseptic solution contained in an integral reservoir with a frangible cover. Spikes affixed to a recess in the sponge pierce the cover to release the solution. The disadvantage of this device and other devices that include liquid-containing ampoules, such as those described in U.S. Patent Nos. 3,89l,33l and 4,l83,684, is the absence of a means to control the delivery of fluid to the sponge. The absence of a means to control the fluid flow rate to the sponge limits the volume of solution that can be delivered without dripping.
- U.S. Patent No. 4,342,522 describes a roll-on dispenser which includes a porous open-cell foam membrane deformable by an applicator ball to regulate the dispensation of controlled amounts of powders. The amount of material dispensed is dependent upon the porosity of the membrane and the porosity of the membrane is dependent upon the degree of its deformation by the ball upon operation of the dispenser.
- This invention relates to an article useful as a dispenser for the application of a liquid to a surface comprising
- (a) a hollow elongate member having a major orifice at one end;
- (b) a layer of unfoamed porous metering material disposed over the major orifice of the hollow elongate member, the porous metering material having a reservoiring capacity of less than about 5.0 cc/gm and the layer capable of regulating the flow of liquid therethrough;
- (c) a layer of sponge material disposed over the exterior surface of the layer of porous metering material; and
- (d) an air vent in the hollow elongate member capable of providing air flow between the exterior and interior of the hollow elongate member.
- The current invention provides a means to reliably deliver in a short period of time a surgical prep solution to an applicator sponge without dripping. The applicator of the present invention controls the flow rate of liquid therein to the applicator sponge without the need for external operator manipulation. Unlike the devices of the prior art, the applicator of this invention provides control of the flow rate of liquid to the applicator sponge without squeezing the liquid container or compressing the applicator sponge. Although intended to apply modern, low viscosity, non-water soluble, film-forming prep solutions, this device can be configured to apply a variety of solution compositions, viscosities and volumes without compromising the fast wetting and no dripping features. The geometry of the device was designed to be compatible with modern antiseptic techniques. Because fabrication of the device utilizes high volume production processes, the manufacturing costs of the device are sufficiently inexpensive to permit disposable use.
-
- Figure l is a perspective view of a preferred applicator of this invention;
- Figure 2 is a cross-section side view of the various unassembled elements of the preferred applicator of Figure l, excluding reservoir l;
- Figure 3 is a cross-section auxiliary view of the top portion of the hollow elongate member shown in Figure 2;
- Figure 4 is a cross-section of the dispensing end of the assembled applicator of Figure l; and
- Figure 5 is a perspective view of a preferred porous metering insert.
- With reference to Figures l and 2, the
applicator 30 includes a reservoir l containing the solution to be applied by the applicator, and a hollowelongate member 24 which acts as a handle and a conduit through which the solution passes before it is dispensed byfoam sponge 8. Preferably, hollowelongate member 24 is bounded by major orifice ll at one end and flange at the opposite end. It is constructed so as to include a fixation means 4 adjacent orifice ll for engaging at orifice ll reservoir l, a tubular handle 3 communicating between major orifice ll andmajor orifice 20 defined byflange 5, and an air vent 9. Air vent 9 aspirates air into hollowelongate member 24 as liquid flows out throughmajor orifice 20 during the dispensation process, thereby maintaining atmospheric pressure inside the applicator. - A
porous metering insert 6 is disposed overmajor orifice 20 and is sandwiched between the underside offlange 5 and open-cell foam sponge 8. Theporous metering insert 6 is disposed overmajor orifice 20 to control the flow of liquid out of hollowelongate member 24 and intofoam sponge 8. -
Foam sponge 8 can be selected from a variety of commercially available materials having a wide range of compression set ratios (i.e., density) and porosities. By varying the pore size, void fraction and hydrophilicity of theporous metering insert 6 and the compression set ratio and porosity of thefoam sponge 8, applicators can be constructed to apply a variety of solution compositions, viscosities and volumes. The pore size, void volume fraction, and hydrophilicity ofporous metering material 6 and the compression set ratio and porosity of open-cell foam sponge 8 are adjusted in relation to the viscosity, volume and surface tension of the liquid to be dispensed to allow a portion of the liquid contained in the applicator to flow to the outer surface ofsponge 8 but not to allow the liquid to drip from the open-cell foam sponge 8 when it is suspended in mid-air withflange 5 down. It should be noted that to create a completely dripless applicator the amount of liquid to be dispensed by the device must not exceed the reservoiring capacity ofsponge 8. - Metering
insert 6 andsponge 8 are held together and disposed overmajor orifice 20 by a variety of suitable means, including adhesive bonding. In the preferred embodiment,elongate member 24 includes aflange 5 surroundingmajor orifice 20. The inner portion offlange 5 contains two lips defined by recesses l3 and l4.Metering insert 6 is contained within recess l3 and is held therein byfoam sponge insert 8 which is adhered to the outer rim offlange 5 by heat-activatable bonding insert 7. - The invention will now be more particularly described in terms of the following preferred embodiment.
- Figure l shows the preferred embodiment fully assembled from each of the parts shown in Figure 2. The device illustrated in Figure l consists of the following components as shown in Figure 2: reservoir l containing the prep solution and sealed at its major orifice 2l by seal 2; hollow
elongate member 24 being threaded at one end to accept reservoir l, and having anangled flange 5 at the opposite end, and including air vent 9;porous metering insert 6 disposed withinflange 5; thermoplastic bonding insert 7 also disposed withinflange 5; andfoam sponge 8. - Reservoir l is preferably a bottle with a threaded opening molded from a thermoplastic material compatible with the prep solution. The preferred embodiment comprises an essentially rigid, high-density polyethylene, cylindrical bottle with threaded portion l0 smaller in diameter than the main body of the bottle. Reservoir l is preferably filled and inductively sealed with foil seal 2 using conventional techniques.
- Hollow
elongate member 24 can be molded from any thermoplastic compatible with the liquid to be dispensed. Preferably, hollowelongate member 24 is molded from medium density polyethylene. Features of the preferred embodiment of this component include tubular handle 3, major orifice ll which communicates with reservoir l at orifice 2l thereof, integrally-formed radially-projecting interior flange l2 which acts as a reservoir seat, integrally-formed fixation means 4 which threadably engages reservoir l, projecting means l9 to tear seal 2 on reservoir l, air vent 9, andflange 5 located at the opposite end of hollowelongate member 24 from orifice ll. - For surgical prep applications it is important that tubular handle 3 be long enough to prevent contact of the patient by the person applying the surgical prep solution. Preferably for such applications tubular handle 3 is at least about four inches long.
- Projecting means l9 is positioned within
hollow elongate member 24 so as to be capable of puncturing seal 2 on reservoir l when reservoir l is engaged at orifice ll by fixation means 4. Many different geometries are possible for projecting means l9. The preferred embodiment, as shown in Figure 3, includes an integrally-formed projection that first extends radially from integrally-formed radially-projecting interior flange l2 and then extends in a direction towards orifice ll, parallel to the longitudinal axis ofelongate member 24. The projection l9 is preferably of a size sufficient to begin rupturing seal 2 after reservoir l has been threaded at least one-half turn into hollowelongate member 24, with complete rupturing occuring three-fourth turn thereafter. Other possible embodiments of projecting means l9 include a hollow metal or polymeric spike. - Air vent 9 is a necessary component of the applicator.
Metering insert 6 greatly restricts the amount of air which can enter the applicator throughorifice 20. In order to avoid creating a vacuum and restricting flow through the device a means of maintaining atmospheric pressure in the device must be employed. Air vent 9 provides such a means. Air vent 9 is preferably an L-shaped slot having its long leg lying parallel to the longitudinal axis ofelongate member 24 and recessed through the threads of fixation means 4, and its short leg lying perpendicular to the longitudinal axis ofelongate member 24 and recessed through an upper portion of interior flange l2. Preferably, air vent 9 is located on the wall of hollowelongate member 24 which forms an obtuse angle withflange 5. In this manner, the liquid runs down the side of tubular handle 3 which is furthest from air vent 9 when the applicator is inverted in the position shown in Figure l. This location of air vent 9 minimizes the potential for leakage when the applicator is moved into position for use. - Further, the short leg of air vent 9 projects only through an upper portion of flange l2, leaving the lower portion of this flange intact and radially projecting into the interior of
elongate member 24. In this manner when the applicator is inverted from the position shown in Figure l and the liquid is allowed to flow from tubular handle 3 back into reservoir l, the liquid cascades over flange l2 and past air vent 9, thereby minimizing the potential for leakage of liquid through air vent 9. As a further means of reducing the potential of leakage, the size of air vent 9 is minimized. - Other geometries and locations of air vent 9 are envisioned by the inventor. For example the air vent could merely comprise a hole through tubular handle 3. Preferably such a hole would not be present in a location which would result in leakage of liquid from the device.
- Preferably
flange 5 is integrally formed and is angled from the longitudinal axis ofelongate member 24 by between about 30 and 90 degrees. Most preferably there is about a 45 degree angle betweenflange 5 and the longitudinal axis ofelongate member 24.Flange 5 preferably includes recesses l3 and l4 on its interior surface. Recesses l3 and l4 are dimensioned and shaped to permit nesting therein ofmetering insert 6 and bonding insert 7, respectively. Preferably recess l4 is greater in area than recess l3 to provide for sandwiching ofmetering insert 6 betweenorifice 20 and bonding insert 7. - The distribution and rate of delivery of the liquid to open-
cell foam sponge 8 is controlled byporous metering insert 6. For a given volume, viscosity, and surface tension of the liquid, rapid wetting of the foam sponge without dripping can be accomplished by appropriate specification of the average pore size, void volume fraction and hydrophilicity ofporous metering insert 6 and the permanent compression set ratio and porosity of open-cell foam sponge 8. - Preferably, the pore size, void volume and hydrophilicity of
porous metering insert 6 are adjusted so that for any given volume, viscosity and surface tension of the liquid to be applied the average flow rate of the liquid throughmetering insert 6 is between about 0.25 and l0 mls/sec. Greater flow rates than this will tend to result in an applicator which drips, while lower flow rates will result in an applicator which does not provide adequate liquid for surgical scrub applications. Most preferably for surgical scrub applications, the average flow rate of liquid throughporous metering insert 6 is between l and 5 ml/sec. In general, for lower volumes and/or higher viscosity liquids the pore size and/or void volume ofporous metering insert 6 is adjusted upwards to achieve the desired flow rates. Furthermore, as the surface tension of the liquid increases the metering insert is varied from a hydrophobic to a hydrophilic material to achieve the desired flow rate. -
Porous metering insert 6 is substantially rigid and can be constructed from either hydrophilic or hydrophobic materials depending upon the liquid to be dispensed.Metering insert 6 can be in the form of sintered metal or plastic, molded unfoamed porous plastic, porous plastic films, porous metal structures and porous ceramics. Methods for making such porous structures include well-known sintering or leaching processes. Preferably, porous metering inserts are constructed from ceramics or thermoplastic materials such as polypropylene, polyethylene, polyvinylidene fluoride, ethylene-vinyl acetate copolymers, styrene-acrylonitrile copolymers and polytetrafluoroethylene. The hydrophilicity of the metering insert can be increased by various well-known treatments. - In general, the average pore size of
metering insert 6 is between about l and 2,000 microns and the void volume is between about l0 and 70 percent. Preferably, for surgical applications where antiseptic solutions are dispensed, the average pore size of the metering insert is between about l0 and 500 microns and the void volume is between about 20 and 60 percent. Most preferably for such applications the average pore size is between about 60 and l00 microns and the void volume is between about 30 and 50 percent. A preferred ceramic material for use as a porous metering insert is 3M Brand Porous Structures™, commercially available from 3M, Saint Paul, Minnesota. This material has an average pore size of between about l4 and l75 microns and a void volume of approximately 30 percent. A particularly preferred porous metering material is a porous high density polyethylene commercially available as Interflo® Porous Plastic, F/N35-l60-22, from Chromex Chemical Corp., Brooklyn, New York. This material has an average pore size of between about 60 and l00 microns and a void volume of between about 40 and 60 percent. In general,metering insert 6 is relatively non-reservoiring, having a reservoiring capacity of less than about 5.0 cc/gm, preferably less than about l.0 cc/gm, and most preferably about 0.7 cc/gm. Fluid which is reservoired in an intermediate flow regulator is not available for application to the surface to be treated. Thus,metering insert 6 provides controlled flow of fluid without significant fluid waste due to retained fluid within the metering insert itself. - As shown most clearly in Figures 4 and 5, the preferred embodiment of
porous metering insert 6 has an area which is greater than the area ofmajor orifice 20. Preferably, the area ofinsert 6 is at least two times greater than the area oforifice 20, and is most preferably almost as large asfoam sponge 8. The preferred embodiment ofmetering insert 6 also has a raised periphery l6 which extends above planar metering area l5 and creates a cavity between active metering area l5 andmajor orifice 20. Preferably, raised periphery l6 extends above planar metering area l5 to the extent of one to two times the thickness of planar metering area l5. Both the increased area ofinsert 6 and raised periphery l6 serve to increase the area of fluid distribution to open-cell foam sponge 8. - Bonding insert 7 is a gasket-like structure, preferably having a rectangular annular shape. Preferably a bridging member 22 is included between opposing sides of bonding insert 7 to provide stuctural support to
foam sponge 8 and prevent sagging thereof due to the weight of the absorbed fluid to be dispensed. - With reference to Figure 4, after assembly of the applicator and inductive melting of bonding insert 7,
metering insert 6 andfoam sponge 8 are peripherally affixed toflange 5 by bond l7, andmetering insert 6 andfoam sponge 8 are bonded together at bond l8. - Bonding insert 7 can be molded, extruded or die cut from a compatible thermoplastic or heat-activatable material filled with an inductively active material. Examples include laminated composites comprised of metal foil sandwiched between layers of thermoplastic or heat-activatable bonding material, such as polyethylene or hot-melt adhesives. Preferred examples include such thermoplastic or heat-activatable bonding materials filled with an inductive metal or metal oxide powder, e.g., 5 to 50 percent by volume iron powder having an average particle size of from about 300 to 400 mesh. A particularly preferred bonding insert 7 is a rigid gasket formed from injection molded polyethylene filled with about l2 to l5 percent by volume iron powder, commercially available from Emabond Inc., Norwood, New Jersey, as G-l0-205.
- Open-
cell foam sponge 8 comprises an open-cell foam material compatible with the liquid to be dispensed. Suitable open-cell foam sponge materials are prepared from elastomeric thermoplastic materials such as polyethylene and polyurethane. Especially preferred open-cell foam materials are prepared from polyurethane elastomers. - By utilizing a permanently compression-set foam, the wicking and reservoiring properties of the
foam sponge 8 can be selected such that the fluid delivered throughmetering insert 6 wets foamsponge 8 but does not drip fromsponge 8 when it is suspended in mid-air withflange 5 down. The greater the compression set ratio, the greater the amount of liquid that can be absorbed by the sponge material. Preferably, the foam sponge material is compression set (i.e., compressed) by heat and pressure to from about l.5 to l0 times its original density, i.e., the compression set ratio is between about l.5 and l0. Most preferably the compression set ratio ofsponge 8 is between about 2 and 4. - The porosity of the foam sponge material can be selected such that
foam sponge 8 will release a uniform amount of liquid when it is lightly rubbed against the surface upon which the liquid is to be dispensed. Preferably, for surgical prep applications, the porosity of the foam sponge material is between about l0 and l00 pores per linear inch, more preferably about 90 pores per linear inch. A particularly preferred open-cell foam sponge material is an elastomeric polyurethane foam having a compression set ratio of between about 2 and 4 and a porosity of about 90 pores per linear inch, commercially available from Scotfoam Corp., Eddystone, Pennsylvania, as Scottfelt™ 3-900-Z. - The applicator of this invention is useful in dispensing liquids having viscosities at ambient temperatures of less than about l0,000 cps, most preferably less than about 500 cps.
- As noted above, the applicator is useful in dispensing antiseptic liquids to cleanse a surgical field prior to surgery. Examples of suitable antiseptic preparations include those described in U.S. application Serial No. 6l7,255, filed June 4, l984, and those described in U.S. 4,542,0l2, the disclosures of which are incorporated herein by reference. The antiseptic liquid is placed in the applicator and the applicator head is gently rubbed over the surgical field to thereby cleanse it. The applicator can be handled easily without dripping the liquid onto other articles in the vicinity of the surgical field. The dripless feature allows application of the liquid to only the desired areas of the patient and also allows for quicker and more efficient use of a surgical facility due to elimination of the time needed to clean the facility of the drippings of antiseptic prep.
- Although specific embodiments of the invention have been described herein, it is not intended to limit the invention solely thereto, but to include all of the obvious variations and modifications within the spirit and scope of the appended claims.
Claims (7)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US79898985A | 1985-11-18 | 1985-11-18 | |
US798989 | 1985-11-18 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0232596A1 true EP0232596A1 (en) | 1987-08-19 |
EP0232596B1 EP0232596B1 (en) | 1991-01-16 |
Family
ID=25174770
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP86308960A Expired - Lifetime EP0232596B1 (en) | 1985-11-18 | 1986-11-17 | Liquid applicator |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0232596B1 (en) |
JP (1) | JPS62120860A (en) |
CA (1) | CA1284784C (en) |
DE (1) | DE3676996D1 (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2668371A1 (en) * | 1990-10-31 | 1992-04-30 | Galtier Claude | Device for applying liquid or pasty products |
FR2722695A1 (en) * | 1994-07-22 | 1996-01-26 | Demic Lab Sa | MEDICAL FRICTION FRICTION CUTANE BADIGEONNAGE USTENSILE |
GB2304607A (en) * | 1995-09-01 | 1997-03-26 | Anita Francesca Hunter | Applicator for cosmetic and other skin lotions |
WO1998012122A1 (en) * | 1996-09-17 | 1998-03-26 | The Procter & Gamble Company | Combination of a package having a porous applicator and a fluid product |
EP1618812A1 (en) * | 1999-07-01 | 2006-01-25 | Filtertek, Inc. | Method of reducing the pore size of a semisolid product dispensing head |
US7261701B2 (en) * | 2002-10-03 | 2007-08-28 | 3M Innovative Properties Co. | Skin antiseptic composition dispenser and methods of use |
WO2007141146A1 (en) * | 2006-06-07 | 2007-12-13 | Beiersdorf Ag | Kit for the application of fluid preparation |
WO2008138343A1 (en) * | 2007-05-16 | 2008-11-20 | Idt-Form Holding Aps | Coating or treatment by potentially hazardous products, such as liquid nano technology coating products |
US8858484B2 (en) | 2008-12-30 | 2014-10-14 | Otsuka America Pharmaceutical, Inc. | Fluid application device and method |
US8911771B2 (en) | 2004-11-17 | 2014-12-16 | Otsuka America Pharmaceutical, Inc. | Fluid application device and method |
US8979785B2 (en) | 2008-12-30 | 2015-03-17 | Otsuka Pharmaceutical Factory, Inc. | Fluid application device and method |
EP3108922A1 (en) * | 2009-09-15 | 2016-12-28 | Becton, Dickinson and Company | Systems for providing an antiseptic applicator |
CN114748775A (en) * | 2022-03-16 | 2022-07-15 | 李文生 | Device is paintd to face skin virus infection medicine |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP7491551B2 (en) * | 2019-04-25 | 2024-05-28 | コスメディ製薬株式会社 | Applicator 2 for water-soluble sheet preparation |
Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1086705A (en) * | 1953-11-09 | 1955-02-15 | Diffuser-screen buffer adaptable to deformable or piston tubes | |
FR1205411A (en) | 1957-04-17 | 1960-02-02 | Improvements to dispensing and applicator devices for liquid containers | |
US3847151A (en) | 1973-06-04 | 1974-11-12 | Int Paper Co | Liquid dispensing device |
US3891331A (en) | 1974-06-14 | 1975-06-24 | Marion Health & Safety Inc | Unit for dispensing liquid from a frangible ampoule |
US4183684A (en) | 1977-11-29 | 1980-01-15 | Marion Health & Safety, Inc. | Fluid dispensing unit |
US4189245A (en) * | 1978-04-28 | 1980-02-19 | Bennett Robert A | Suction producing disposable pump and dispenser |
US4229116A (en) * | 1979-03-05 | 1980-10-21 | Moore Lee P | Liquid soap dispenser and brush combination |
US4342522A (en) | 1977-03-10 | 1982-08-03 | Bristol-Myers Company | Roll-on dispenser with a flexible membrane |
GB2119235A (en) * | 1982-04-07 | 1983-11-16 | John Christopher Graham | Cleaning device |
US4463880A (en) * | 1982-04-30 | 1984-08-07 | The Regents Of The University Of California | Medicine drop dispenser with anti-bacterial filter |
US4507111A (en) | 1981-03-09 | 1985-03-26 | Whitman Medical Corporation | Surgical scrub |
US4542012A (en) | 1982-07-02 | 1985-09-17 | Minnesota Mining And Manufacturing Company | Film-forming composition containing an antimicrobial agent and methods |
US4584192A (en) | 1984-06-04 | 1986-04-22 | Minnesota Mining & Manufacturing Company | Film-forming composition containing an antimicrobial agent and methods of use |
-
1986
- 1986-10-29 CA CA000521684A patent/CA1284784C/en not_active Expired - Lifetime
- 1986-11-17 DE DE8686308960T patent/DE3676996D1/en not_active Expired - Lifetime
- 1986-11-17 EP EP86308960A patent/EP0232596B1/en not_active Expired - Lifetime
- 1986-11-17 JP JP61273819A patent/JPS62120860A/en active Granted
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1086705A (en) * | 1953-11-09 | 1955-02-15 | Diffuser-screen buffer adaptable to deformable or piston tubes | |
FR1205411A (en) | 1957-04-17 | 1960-02-02 | Improvements to dispensing and applicator devices for liquid containers | |
US3847151A (en) | 1973-06-04 | 1974-11-12 | Int Paper Co | Liquid dispensing device |
US3891331A (en) | 1974-06-14 | 1975-06-24 | Marion Health & Safety Inc | Unit for dispensing liquid from a frangible ampoule |
US4342522A (en) | 1977-03-10 | 1982-08-03 | Bristol-Myers Company | Roll-on dispenser with a flexible membrane |
US4183684A (en) | 1977-11-29 | 1980-01-15 | Marion Health & Safety, Inc. | Fluid dispensing unit |
US4189245A (en) * | 1978-04-28 | 1980-02-19 | Bennett Robert A | Suction producing disposable pump and dispenser |
US4229116A (en) * | 1979-03-05 | 1980-10-21 | Moore Lee P | Liquid soap dispenser and brush combination |
US4507111A (en) | 1981-03-09 | 1985-03-26 | Whitman Medical Corporation | Surgical scrub |
GB2119235A (en) * | 1982-04-07 | 1983-11-16 | John Christopher Graham | Cleaning device |
US4463880A (en) * | 1982-04-30 | 1984-08-07 | The Regents Of The University Of California | Medicine drop dispenser with anti-bacterial filter |
US4542012A (en) | 1982-07-02 | 1985-09-17 | Minnesota Mining And Manufacturing Company | Film-forming composition containing an antimicrobial agent and methods |
US4584192A (en) | 1984-06-04 | 1986-04-22 | Minnesota Mining & Manufacturing Company | Film-forming composition containing an antimicrobial agent and methods of use |
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2668371A1 (en) * | 1990-10-31 | 1992-04-30 | Galtier Claude | Device for applying liquid or pasty products |
FR2722695A1 (en) * | 1994-07-22 | 1996-01-26 | Demic Lab Sa | MEDICAL FRICTION FRICTION CUTANE BADIGEONNAGE USTENSILE |
WO1996003177A1 (en) * | 1994-07-22 | 1996-02-08 | Laboratoires Demic | Novel skin swab device and medical and surgical applications therof |
GB2304607A (en) * | 1995-09-01 | 1997-03-26 | Anita Francesca Hunter | Applicator for cosmetic and other skin lotions |
GB2304607B (en) * | 1995-09-01 | 1999-07-21 | Anita Francesca Hunter | Applicator for cosmetic and other skin-lotions |
WO1998012122A1 (en) * | 1996-09-17 | 1998-03-26 | The Procter & Gamble Company | Combination of a package having a porous applicator and a fluid product |
EP1618812A1 (en) * | 1999-07-01 | 2006-01-25 | Filtertek, Inc. | Method of reducing the pore size of a semisolid product dispensing head |
US7261701B2 (en) * | 2002-10-03 | 2007-08-28 | 3M Innovative Properties Co. | Skin antiseptic composition dispenser and methods of use |
US8911771B2 (en) | 2004-11-17 | 2014-12-16 | Otsuka America Pharmaceutical, Inc. | Fluid application device and method |
WO2007141146A1 (en) * | 2006-06-07 | 2007-12-13 | Beiersdorf Ag | Kit for the application of fluid preparation |
US7874756B2 (en) | 2006-06-07 | 2011-01-25 | Beiersdorf Ag | Kit for the application of a fluid preparation |
CN101466288B (en) * | 2006-06-07 | 2011-11-02 | 拜尔斯道夫股份公司 | Kit for the application of fluid preparation |
WO2008138343A1 (en) * | 2007-05-16 | 2008-11-20 | Idt-Form Holding Aps | Coating or treatment by potentially hazardous products, such as liquid nano technology coating products |
US8858484B2 (en) | 2008-12-30 | 2014-10-14 | Otsuka America Pharmaceutical, Inc. | Fluid application device and method |
US8979785B2 (en) | 2008-12-30 | 2015-03-17 | Otsuka Pharmaceutical Factory, Inc. | Fluid application device and method |
US9566421B2 (en) | 2008-12-30 | 2017-02-14 | Otsuka America Pharmaceutical, Inc. | Fluid application device and method |
EP3108922A1 (en) * | 2009-09-15 | 2016-12-28 | Becton, Dickinson and Company | Systems for providing an antiseptic applicator |
CN114748775A (en) * | 2022-03-16 | 2022-07-15 | 李文生 | Device is paintd to face skin virus infection medicine |
CN114748775B (en) * | 2022-03-16 | 2024-05-03 | 南京曼星忆知科技有限公司 | Facial skin virus infection medicine smearing device |
Also Published As
Publication number | Publication date |
---|---|
EP0232596B1 (en) | 1991-01-16 |
JPH0580911B2 (en) | 1993-11-10 |
DE3676996D1 (en) | 1991-02-21 |
CA1284784C (en) | 1991-06-11 |
JPS62120860A (en) | 1987-06-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4925327A (en) | Liquid applicator with metering insert | |
EP0232596A1 (en) | Liquid applicator | |
EP0671960B1 (en) | Liquid applicator with metering insert | |
US10463844B2 (en) | Dispensing applicator for fluids | |
US5288159A (en) | Liquid applicator with frangible ampoule and support | |
US10363405B2 (en) | Dispensing applicator for fluids | |
CA2428099C (en) | Liquid applicator with diametrically opposed wings | |
US7540681B2 (en) | Surgical prep solution applicator | |
US9220881B2 (en) | Dispensing applicator for fluids | |
WO2007076121A1 (en) | Surgical prep solution applicator | |
US5713843A (en) | Sponge applicator with fluid ball | |
US10478602B2 (en) | Antiseptic swab with activation button | |
US10828477B2 (en) | Dispensing applicator for fluids | |
WO2023172427A1 (en) | Product delivery device system and methods |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): DE FR GB IT SE |
|
17P | Request for examination filed |
Effective date: 19880219 |
|
17Q | First examination report despatched |
Effective date: 19890505 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): DE FR GB IT SE |
|
ITF | It: translation for a ep patent filed | ||
REF | Corresponds to: |
Ref document number: 3676996 Country of ref document: DE Date of ref document: 19910221 |
|
ET | Fr: translation filed | ||
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
EAL | Se: european patent in force in sweden |
Ref document number: 86308960.3 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20001101 Year of fee payment: 15 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20001102 Year of fee payment: 15 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20001103 Year of fee payment: 15 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 20001106 Year of fee payment: 15 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20011117 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20011118 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
EUG | Se: european patent has lapsed |
Ref document number: 86308960.3 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020702 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20011117 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020730 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED. Effective date: 20051117 |